A Newborn Infant with Congenital Central Hypoventilation Syndrome and Pupillary Abnormalities: A Literature Review

We present a neonate with early onset apnea and bradycardia in the absence of primary cardiorespiratory and central nervous system disorders that eventually required chronic ventilator support starting at 6 hours of life. Molecular testing of paired-like homeobox 2b (PHOX2B) gene mutation confirmed...

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Detalles Bibliográficos
Autores principales: Harsono, Mimily, Chilakala, Sandeep, Bohn, Shiva, Pivnick, Eniko K., Pourcyrous, Massroor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers, Inc. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522484/
https://www.ncbi.nlm.nih.gov/pubmed/36187199
http://dx.doi.org/10.1055/a-1883-0140

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522484/
https://www.ncbi.nlm.nih.gov/pubmed/36187199
http://dx.doi.org/10.1055/a-1883-0140

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